NobleAid ACETAMINOPHEN CAPLETS

NobleAid by

Drug Labeling and Warnings

NobleAid by is a Otc medication manufactured, distributed, or labeled by Noble Otc LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NOBLEAID- acetaminophen tablet, film coated 
Noble Otc LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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NobleAid ACETAMINOPHEN CAPLETS

DRUG FACTS

ACTIVE INGREDIENT (in each caplet)

Acetaminophen 500mg

PURPOSE

Pain reliever/fever reducer

Uses

Temporarily relieves minor aches and pains due to:
      Headache            Muscular aches
      Backache            Minor pain of Arthritis
      Common cold      Toothache
      Premenstrual and menstrual cramps
temporarily reduces fever.

Warnings

Liver Warning: This product contains acetaminophen. Severe liver damage may occur
    if you take more than 4,000 mg of acetaminophen in 24 hours
    with other drugs containing acetaminophen
    3 or more alcoholic drinks every day while using this product.

Allergy Alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
Skin reddening    Blisters    rash.
If a skin reaction occurs, stop use and seek medical help right away.

Do not use

with any other drug containing acetaminophen (prescription or nonprescription).
If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a Doctor before use if you have liver disease

Ask a Doctor before use if you are taking the blood thinning drug warfarin

Stop use and ask a doctor if
    pain gets worse or last more than 10 days
    fever gets worse or last more than 3 days
    new symptoms occur redness or swelling is present.
This could be signs of serious condition.

If pregnant or breastfeeding, ask a health professional before use

Keep out of reach of children.
Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Do not take more than directed (see overdose warning)

• Adults & Children 12 years and over: Take 2 caplets every 6 hours while symptoms last.; Do not take more than 6 caplets in 24 hours,; unless directed by a doctor.; Do not use more than 10 days unless directed; by a doctor.
• Children under 12 years: Ask a doctor

Inactive Ingredients

FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, mica-based pearlescent pigment, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, stearic acid.

Other Information

Store at 20-25 C (68-77 F)

ACETAMINOPHEN CAPLETS

EXTRA STRENGTH

RAPID RELEASE PAIN RELIEF

Compare to the Active Ingredient in Tylenol© 

Extra Strength Rapid Release Gels

√ Pain Reliever

√ Fever Reducer

√ Aspirin Free

For Adults

DO NOT USE IF THE PRINTED SEAL UNDER CAP IS BROKEN OR MISSING

Manufactured for
Noble OTC LLC
Perth Amboy NJ 08861
www.nobleotc.com

Packaging

NOBLEAID 
acetaminophen tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81533-500
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MICA (UNII: V8A1AW0880)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	red	Score	no score
Shape	capsule (Caplet)	Size	19mm
Flavor		Imprint Code	500
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81533-500-30	300 in 1 BOTTLE; Type 0: Not a Combination Product	05/10/2021	03/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	05/10/2021	03/31/2023

Labeler - Noble Otc LLC (041836435)

Revised: 7/2022

Document Id: 6983b2fd-9ea0-4bca-9f47-14eadddc94cd

34390-5

Set id: df5c0266-036c-435a-95f0-42d57c7fb8e3

Version: 2

Effective Time: 20220719